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FDA 510(k)

ARTHRO-SURGIMAT

K-Number: K962114 · 1996-08-22

ApplicantW.O.M. World of Medicine GmbH
Decision Date1996-08-22
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ARTHRO-SURGIMAT is the device name listed in this FDA 510(k) record. The listed applicant is W.O.M. World of Medicine GmbH. It received FDA 510(k) clearance on 1996-08-22 under 510(k) number K962114. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHRO-SURGIMAT?

ARTHRO-SURGIMAT is a medical device that received FDA 510(k) clearance on 1996-08-22. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K962114.

When did ARTHRO-SURGIMAT receive FDA 510(k) clearance?

ARTHRO-SURGIMAT received FDA 510(k) clearance on 1996-08-22, under 510(k) number K962114.

Who is the listed applicant for ARTHRO-SURGIMAT?

The FDA 510(k) record lists W.O.M. World of Medicine GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTHRO-SURGIMAT?

The FDA product code for ARTHRO-SURGIMAT is HRX.

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Other records listing W.O.M. World of Medicine GmbH as applicant

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Related Devices (Code: HRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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